HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787401Generated: October 29, 2026
Dimethylformamide → 8-Vinyl-1,4-dioxaspiro[4,5]decane
https://huagongshe.com/reaction/1787401
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 8-(2-Iodoethyl)-1,4-dioxaspiro[4.5]decane | HCID 57598630 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-Vinyl-1,4-dioxaspiro[4,5]decane | HCID 57598919 | 81.5% |
Reaction Steps
Fifth Step: 223.0 g of the compound (14) and 800 mL of DMF were added to a reactor under nitrogen atmosphere, and stirred at 3° C. under cooling with ice. 92.9 g of potassium t-butoxide (t-BuOK) was added thereto by dividing into 10 portions at a temperature range of from 3 to 10° C., followed by further stirring at 0° C. for 3 hours. After confirming that the reaction had been completed by GC analysis, the reaction mixture was poured into and mixed with a mixture of 1,500 mL of heptane and 1,500 mL of water at 0° C. The mixture was separated into an organic layer and an aqueous layer by standing still, so as to attain extraction to the organic layer. The resulting organic layer was fractionated and washed with water, followed by drying over anhydrous magnesium sulfate. The resulting organic layer was purified by silica gel column chromatography using heptane as eluent, and the solvent was removed by distillation under reduced pressure. The resulting residue was distilled under reduced pressure to obtain 103.3 g of 8-vinyl-1,4-dioxaspiro[4,5]decane (15) as a colorless transparent liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07510749B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-f75e17883ca9440191277de326bd4422 |
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| Source note | uspto-grants-2009_03 |
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